K-number	K965076
Device name	MDA HEPARIN ANTI-X ASSAY
Applicant	Organon Teknika Corp.
Product code	KFF
Device class	Class II
Decision date	Mar 18, 1997
Decision	Substantially Equivalent
Regulation	864.7525

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View the full FDA submission: accessdata.fda.gov

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MDA HEPARIN ANTI-X ASSAY

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